| Cat. No. |
Product Name |
Information |
| PC-38655 |
ELOVL1-IN-27
ELOVL1 inhibitor
|
ELOVL1-IN-27 is a highly potent, selective, CNS-penetrant inhibitor of elongation of very long chain fatty acid 1 enzyme (ELOVL1) with IC50 of 13 nM (C26:0 VLCFA inhibition in HEK cell). |
| PC-38598 |
Azo-resveratrol
Tyrosinase inhibitor
|
Azo-resveratrol is a potent mushroom tyrosinase inhibitor with IC50 of 36.28 uM. |
| PC-38531 |
ML266
GCase chaperone
|
ML266 (CID 46943215) is a non-inhibitory chaperone of glucocerebrosidase (GCase) enzyme, does not inhibit the enzyme’s action, but can facilitate its translocation to the lysosome. |
| PC-73312 |
FQI2
LSF inhibitor
|
Factor quinolinone inhibitor 2 (FQI2) is a small molecule inhibitor of transcription factor LSF, inhibits LSF DNA-binding activity both in vitro and in cells (IC50=0.71 uM). |
| PC-73176 |
PPA904
Photosensitizer
|
PPA-904 is a specific phenothiazine photosensitizer in photodynamic therapy (PDT) research, especially topical application for cutaneous leishmaniasis in vivo. |
| PC-73160 |
ALC-0315
Vaccine adjuvant
|
ALC-0315 is a synthetic ionizable amino lipid that has been used in combination with other lipids in the formation of lipid nanoparticles, has attracted attention as a component of the SARS-CoV-2 vaccine. |
| PC-73158 |
JHU37152
DREADD agonist
|
JHU37152 is a high affinity and highly potent activator (agonist) of hM3Dq and hM4Di DREADDs with Ki 1.8 nM and 8.7 nM for hM3Dq and hM4Di in vitro. |
| PC-73146 |
FR 901463
|
FR 901463 is an anti-tumor agent isolated from the fermentation broth of Pseudomonas sp. No. 2663. |
| PC-72942 |
BRM011
BRM/BRG1 inhibitor
|
BRM011 (dual BRM and BRG1 inhibitor 11) is a potent, selective, allosteric dual BRM and BRG1 inhibitor with IC50 of <5 nM for both. |
| PC-72856 |
PUS7 inhibitor C17
PUS7 inhibitor
|
PUS7 inhibitor C17 is a small molecule inhibitor of pseudouridine synthase PUS7, preferentially targets glioblastoma stem cells (GSCs) compared to NSCs. |
| PC-72761 |
UbV SP.3
STAMBP inhibitor
|
UbV SP.3 is potent, selective inhibitor of STAMBP isopeptidase activity with KD/IC50 of 60/9.8 nM, with significant preferential binding to STAMBP over STAMBPL1 (250 -fold selectivity). |
| PC-72760 |
UbV SP.1
STAMBP inhibitor
|
UbV SP.1 is potent, selective inhibitor of STAMBP isopeptidase activity with KD of 0.05/0.18 uM for STAMBP/STAMBPL1, respectively. |
